Catalog Number

AB-00050

Brand Name

ARROW

Version/Model Number

IPN040000

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K121403,K121403,K121403

Product Code

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

b465ff23-a5d4-478d-b0f0-9fe13154a5a5

Public Version Date

June 15, 2021

Public Version Number

6

DI Record Publish Date

January 10, 2017

Package DI Number

50801902124673

Quantity per Package

1

Contains DI Package

70801902124677

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case